Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G Sankaran

Showing results (221-230 of 240) with videos related to

Pageof 24
Sort By:
The Journal of Allergy and Clinical Immunology|September 27, 2020
Coronavirus disease 2019 in patients with inborn errors of immunity: An international studyIsabelle Meyts, Giorgia Bucciol, Isabella Quinti, et al.
Nature Communications|November 27, 2025
Human plasma proteomic profile of clonal hematopoiesisZhi Yu, Amélie Vromman, Ngoc Quynh H Nguyen, et al.
American Journal of Human Genetics|September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
American Journal of Human Genetics|August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
American Journal of Human Genetics|April 2, 2024
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Genomic and phenotypic correlates of mosaic loss of chromosome Y in bloodYasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
American Journal of Human Genetics|January 14, 2025
Genomic and phenotypic correlates of mosaic loss of chromosome Y in bloodYasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Medrxiv : the Preprint Server for Health Sciences|February 8, 2024
Unique Capabilities of Genome Sequencing for Rare Disease DiagnosisMonica H Wojcik, Gabrielle Lemire, Maha S Zaki, et al.
Pageof 24

Showing results (221-230 of 240) with videos related to

Sort By:
Pageof 24
The Journal of Allergy and Clinical Immunology|September 27, 2020
Coronavirus disease 2019 in patients with inborn errors of immunity: An international studyIsabelle Meyts, Giorgia Bucciol, Isabella Quinti, et al.
Nature Communications|November 27, 2025
Human plasma proteomic profile of clonal hematopoiesisZhi Yu, Amélie Vromman, Ngoc Quynh H Nguyen, et al.
American Journal of Human Genetics|September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
American Journal of Human Genetics|August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
American Journal of Human Genetics|April 2, 2024
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Genomic and phenotypic correlates of mosaic loss of chromosome Y in bloodYasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
American Journal of Human Genetics|January 14, 2025
Genomic and phenotypic correlates of mosaic loss of chromosome Y in bloodYasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Medrxiv : the Preprint Server for Health Sciences|February 8, 2024
Unique Capabilities of Genome Sequencing for Rare Disease DiagnosisMonica H Wojcik, Gabrielle Lemire, Maha S Zaki, et al.
Pageof 24